Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Phenotypic and genetic analysis of a child with partial trisomy 7q].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 10 May 2023

Wang Chaojie, Li Dongxiao, Zhang Yaodong, Kong Jinghui, Li Rui, Gao Chao, Shang Qing, Zhang Huichun

Abstract excerpt

OBJECTIVE: To define the nature and origin of a chromosomal aberration in a child with unexplained growth and development retardation, and to analyze its genotype-phenotype correlation. METHODS: A child who had presented at the Affiliated Children's Hospital of Zhengzhou University on July 9, 2019 was selected as the study subject. Chromosomal karyotypes of the child and her parents were determined with routine...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosome Banding
Share to Chromosomes, Human, Pair 7

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Karyotyping

Share to Phenotype

Share to Trisomy

Source

Identifiers

PMID: 37102298
DOI: 10.3760/cma.j.cn511374-20220415-00252

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Phenotypic and genetic analysis of a child with partial trisomy 7q].PMID 37102298Read ↗

[Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].Semantic proximity Read ↗

[Genetic analysis of a child with Sotos syndrome].Semantic proximity Read ↗

[Clinical phenotype and genetic analysis of a child with partial duplication of 10q and a literature review].Semantic proximity Read ↗

A boy with partial trisomy of chromosome 3q24-q28 from paternal balanced insertion and multiple congenital anomalies.Semantic proximity Read ↗

[Phenotypic and genetic analysis of a child featuring multiple malformations due to chromosome 14q deletion].Semantic proximity Read ↗

[Genetic study of a child with developmental delay and mental retardation].Semantic proximity Read ↗

[Phenotypic and genetic analysis of a boy with partial trisomy of 1q].Semantic proximity Read ↗

[Genetic analysis of a child with mental retardation and hypospadia].Semantic proximity Read ↗

[Phenotypic and genetic analysis of a boy with 3p26.3-pter deletion and 7q31.33-qter duplication].Semantic proximity Read ↗

[Clinical and genetic analysis of a child with X-linked mental retardation due to variant of SLC9A7 gene].Semantic proximity Read ↗

[Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient].Semantic proximity Read ↗

[Application of SNP-array technology in the genetic analysis of pediatric patients with growth retardation].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.